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机构地区:[1]郑州大学基础医学院生物化学与分子生物学教研室,郑州450001
出 处:《郑州大学学报(医学版)》2012年第6期807-810,共4页Journal of Zhengzhou University(Medical Sciences)
摘 要:目的:探讨表没食子儿茶素没食子酸酯(EGCG)对人肺腺癌细胞株A549细胞增殖、凋亡及人端粒酶逆转录酶(hTERT)表达的影响。方法:用0、50、100、150、200、250mg/LEGCG分别作用A549细胞24、48和72h后,MTT比色法检测细胞增殖抑制率;0、100、200、250mg/LEGCG干预48h后,应用AnnexinV-FITC/PI双染法检测A549细胞的凋亡情况,应用RT-PCR和免疫细胞化学分别检测细胞内hTERTmRNA和蛋白的表达。结果:EGCG可抑制A549细胞的增殖,并随着剂量增加和时间延长,抑制率增加(F组间=185.944,F时间=291.234,F交互=4186.119,P均<0.001)。EGCG促进A549细胞凋亡(F=2757.183,P<0.001),还可抑制A549细胞中hTERTmRNA与蛋白的表达(F=260.861和953.327,P均<0.001)。结论:EGCG能有效地抑制A549细胞的增殖,诱导其凋亡,其机制可能与下调hTERT的表达有关。Aim:To investigate the effects of epigallocatechin-3-gallate(EGCG)on proliferation and apoptosis and the expression of human telomerase reverse transcriptase(hTERT)of human lung adenocarcinoma cell line A549.Methods:A549 cells were treated with 0,50,100,150,200,250 mg/L EGCG for 24,48,and 72 h,respectively.MTT assay was used to detect the inhibitory rate of cell proliferation.Flow cytometry with Annexin V-FITC/PI double staining was employed to analyze the apoptosis of A549 cells treated with various concentrations of EGCG(0,100,200,250 mg/L)for 48 h,and RT-PCR and immunocytochemistry were applied to detect the mRNA and protein expression of hTERT.Results:EGCG inhibited the cell proliferation of A549 in a dose dependent manner(Fgroup=185.944,Ftime=291.234,Finteraction=4 186.119,P0.001),and promoted the apoptosis of A549 cells(F=2 757.183,P0.001).EGCG could suppress the mRNA and protein expression of hTERT(F=260.861 and 953.327,P0.001).Conclusion:EGCG can effectively inhibit cell proliferation and induce apoptosis of A549 cells,which may be associated with downregulation of hTERT expression.
关 键 词:表没食子儿茶素没食子酸酯 人端粒酶逆转录酶 肺肿瘤 A549细胞
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